Enhanced long-term synaptic depression in an animal model of depression

Biol Psychiatry. 2007 Jul 1;62(1):92-100. doi: 10.1016/j.biopsych.2006.07.007. Epub 2006 Dec 4.


Background: A growing body of evidence suggests a disturbance of brain plasticity in major depression. In contrast to hippocampal neurogenesis, much less is known about the role of synaptic plasticity. Long-term potentiation (LTP) and long-term depression (LTD) regulate the strength of synaptic transmission and the formation of new synapses in many neural networks. Therefore, we examined the modulation of synaptic plasticity in the chronic mild stress animal model of depression.

Methods: Adult rats were exposed to mild and unpredictable stressors for 3 weeks. Thereafter, long-term synaptic plasticity was examined in the hippocampal CA1 region by whole-cell patch clamp measurements in brain slices. Neurogenesis was assessed by doublecortin immunostaining.

Results: Exposure to chronic mild stress facilitated LTD and had no effect on LTP. Chronic application of the antidepressant fluvoxamine during the stress protocol prevented the facilitation of LTD and increased the extent of LTP induction. Neurogenesis in the dentate gyrus was impaired after chronic stress.

Conclusions: In addition to neurogenesis, long-term synaptic plasticity is an important and ubiquitous form of brain plasticity that is disturbed in an animal model of depression. Facilitated depression of synaptic transmission might impair function and structure of brain circuits involved in the pathophysiology of major depression. Antidepressants might counteract these alterations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chronic Disease
  • Dentate Gyrus / physiology
  • Depressive Disorder / drug therapy
  • Depressive Disorder / physiopathology*
  • Disease Models, Animal*
  • Fluvoxamine / pharmacology
  • Hippocampus / physiopathology
  • Long-Term Potentiation / physiology
  • Long-Term Synaptic Depression / physiology*
  • Neuronal Plasticity / physiology*
  • Patch-Clamp Techniques
  • Rats
  • Rats, Wistar
  • Stress, Psychological / physiopathology*
  • Synaptic Transmission / physiology*


  • Fluvoxamine